Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs563539429 0.851 0.240 9 136677540 missense variant C/A;G;T snv 4.1E-06; 8.1E-06; 1.5E-03 5
rs606231168 0.925 0.120 9 136676681 splice acceptor variant C/G snv 4.0E-06 7.0E-06 2
rs764260414 0.925 0.120 9 136677440 missense variant C/T snv 8.0E-06 1.4E-05 2
rs104894093 1.000 0.120 9 136677537 stop gained G/A snv 1.6E-05 1.4E-05 1
rs104894100 1.000 0.120 9 136673906 missense variant A/G snv 1
rs1057517649 1.000 0.120 9 136677558 splice acceptor variant T/C snv 1
rs1057517650 1.000 0.120 9 136687175 splice donor variant C/T snv 1
rs1057517651 1.000 0.120 9 136677545 stop gained C/T snv 1
rs1057517653 1.000 0.120 9 136676635 frameshift variant C/- delins 1
rs1057517654 1.000 0.120 9 136674733 splice donor variant A/C snv 1
rs1057517655 1.000 0.120 9 136673913 stop gained G/A snv 1
rs1057517656 1.000 0.120 9 136673826 inframe deletion TCCTCATGG/- delins 1
rs1057518714 1.000 0.120 9 136676670 stop gained C/T snv 1
rs116807569 1.000 0.120 9 136674809 splice acceptor variant T/C snv 1.0E-04 4.2E-04 1
rs121908925 1.000 0.120 9 136674753 stop gained T/A snv 1
rs121908926 1.000 0.120 9 136676603 stop gained G/A;T snv 1.6E-05 1
rs138994150 1.000 0.120 9 136674750 stop gained T/A snv 4.0E-04 1.0E-03 1
rs145975461 1.000 0.120 9 136673873 missense variant G/A;C snv 8.4E-04; 4.3E-06; 4.3E-06 1
rs1564290079 1.000 0.120 9 136674770 frameshift variant GGAGA/- delins 1
rs1564290914 1.000 0.120 9 136676660 frameshift variant G/- delins 1
rs200656731 1.000 0.120 9 136673876 missense variant G/A;C snv 7.3E-05; 2.6E-05 1
rs387906355 1.000 0.120 9 136677075 frameshift variant -/A delins 8.0E-06 7.7E-05 1
rs387906356 1.000 0.120 9 136677033 inframe deletion AGA/- delins 7.0E-06 1
rs541978825 1.000 0.080 9 136676673 missense variant A/G snv 2.4E-05 1
rs748157664 1.000 0.120 9 136676659 stop gained C/A;T snv 4.0E-06; 8.0E-06 1